FDA Inspection 1308980 — Groman, Inc.

Groman, Inc. — FEI 3004361444

The FDA completed an inspection of Groman, Inc. on March 17, 2026 in Margate, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 17, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Margate, FL (United States)